Raj Kumar Tak
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View article: α-Bromoacetate as a Mild and Safe Brominating Agent in the Light-Driven Vicinal Dibromination of Unactivated Alkenes and Alkynes
α-Bromoacetate as a Mild and Safe Brominating Agent in the Light-Driven Vicinal Dibromination of Unactivated Alkenes and Alkynes Open
Light-induced vicinal dibromination of unactivated alkenes and alkynes has been demonstrated by using methyl α-bromoacetate as a mild brominating agent. A near-visible light (370 nm) light-emitting diode (LED) mediates this simple dibromin…
View article: α-Bromoacetate as a Mild and Safe Brominating Agent in the Light-Driven Vicinal Dibromination of Unactivated Alkene and Alkynes
α-Bromoacetate as a Mild and Safe Brominating Agent in the Light-Driven Vicinal Dibromination of Unactivated Alkene and Alkynes Open
Light-induced vicinal dibromination of unactivated alkenes and alkyne has been demonstrated by using methyl alpha-bromoacetate as a mild brominating agent. Near-visible light (370 nm) light-emitting diode (LED) mediates this simple dibromi…
View article: Synthesis of Tetra‐Substituted 3‐Hydroxyphthalide Esters by Isothiourea‐Catalysed Acylative Dynamic Kinetic Resolution
Synthesis of Tetra‐Substituted 3‐Hydroxyphthalide Esters by Isothiourea‐Catalysed Acylative Dynamic Kinetic Resolution Open
A general and highly enantioselective method for the preparation of tetra‐substituted 3‐hydroxyphthalide esters via isothiourea‐catalysed acylative dynamic kinetic resolution (DKR) is reported. Using (2 S ,3 R )‐HyperBTM (5 mol %) as the c…
View article: Synthesis of Tetra‐Substituted 3‐Hydroxyphthalide Esters by Isothiourea‐Catalysed Acylative Dynamic Kinetic Resolution
Synthesis of Tetra‐Substituted 3‐Hydroxyphthalide Esters by Isothiourea‐Catalysed Acylative Dynamic Kinetic Resolution Open
A general and highly enantioselective method for the preparation of tetra‐substituted 3‐hydroxyphthalide esters via isothiourea‐catalysed acylative dynamic kinetic resolution (DKR) is reported. Using (2 S ,3 R )‐HyperBTM (5 mol %) as the c…
View article: Catalytic Photoredox Carbobromination of Unactivated Alkenes with α-Bromocarbonyls via the Mechanistically Distinct Radical-Addition Radical-Pairing Pathway
Catalytic Photoredox Carbobromination of Unactivated Alkenes with α-Bromocarbonyls via the Mechanistically Distinct Radical-Addition Radical-Pairing Pathway Open
We disclose a catalytic photoredox carbobromination of unactivated alkenes with α-bromocarbonyl compounds under a blue LED light. The reaction proceeds with α-bromoesters, α-bromonitriles and α-bromo-γ-lactones along with terminal and 1,2-…
View article: Enantioselective Synthesis of Tetra-substituted 3-Hydroxyphthalide Esters by Isothiourea-Catalysed Acylative Dynamic Kinetic Resolution
Enantioselective Synthesis of Tetra-substituted 3-Hydroxyphthalide Esters by Isothiourea-Catalysed Acylative Dynamic Kinetic Resolution Open
A general and highly enantioselective method for the preparation of tetra-substituted 3-hydroxyphthalide esters via isothiourea-catalysed acylative dynamic kinetic resolution (DKR) is reported. Using (2S,3R)-HyperBTM (5 mol%) as the cataly…
View article: Catalytic Photoredox Carbobromination of Unactivated Alkenes with a-Bromocarbonyls via Mechanistically Distinct Radical-Addition Radical-Pairing Pathway
Catalytic Photoredox Carbobromination of Unactivated Alkenes with a-Bromocarbonyls via Mechanistically Distinct Radical-Addition Radical-Pairing Pathway Open
We disclose a catalytic photoredox carbobromination of unactivated alkenes with -bromocarbonyl compounds under a blue LED light. The reaction proceeds with -bromoesters, -bromonitriles and -bromo--lactones along with terminal and 1,2-disub…
View article: Catalytic Photoredox Carbobromination of Unactivated Alkenes with a-Bromocarbonyls via Mechanistically Distinct Radical-Addition Radical-Pairing Pathway
Catalytic Photoredox Carbobromination of Unactivated Alkenes with a-Bromocarbonyls via Mechanistically Distinct Radical-Addition Radical-Pairing Pathway Open
We disclose a catalytic photoredox carbobromination of unactivated alkenes with -bromocarbonyl compounds under a 390 nm LED light. The reaction proceeds with -bromoesters, -bromonitriles and -bromo--lactones along with terminal and 1,2-dis…
View article: CCDC 2224825: Experimental Crystal Structure Determination
CCDC 2224825: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2224828: Experimental Crystal Structure Determination
CCDC 2224828: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2224826: Experimental Crystal Structure Determination
CCDC 2224826: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: Photosensitized O <sub>2</sub> enables intermolecular alkene cyclopropanation by active methylene compounds
Photosensitized O <sub>2</sub> enables intermolecular alkene cyclopropanation by active methylene compounds Open
Cyclopropanes are key features in many preclinical, clinical, and commercial drugs, as well as natural products. The most prolific technique for their synthesis is the metal-catalyzed reaction of an alkene with a diazoalkane, a highly ener…
View article: Photosensitized Dioxygen Enables Intermolecular Cyclopropanation of Alkenes Directly with Active Methylene Compounds
Photosensitized Dioxygen Enables Intermolecular Cyclopropanation of Alkenes Directly with Active Methylene Compounds Open
Cyclopropane, a versatile synthetic intermediate, is forged as a key structural feature in many preclinical, clinical and commercial drugs, and occur as a skeletal motif in numerous natural products. The most prolific technique for its syn…
View article: CCDC 2145423: Experimental Crystal Structure Determination
CCDC 2145423: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2145421: Experimental Crystal Structure Determination
CCDC 2145421: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: Cu-Catalyzed Cyclization/Coupling of Alkenyl Aldimines. Indolization of Aldehydes, Anilines and Arylzinc Reagents
Cu-Catalyzed Cyclization/Coupling of Alkenyl Aldimines. Indolization of Aldehydes, Anilines and Arylzinc Reagents Open
We report a Cu(II)-catalyzed cyclization/coupling of alkenyl aldimines with arylzinc reagents to create complex indole-3-diarylmethane derivatives. The aldimines are readily available by simple dehydration, making the process a formal thre…
View article: CCDC 2049408: Experimental Crystal Structure Determination
CCDC 2049408: Experimental Crystal Structure Determination Open
View article: CCDC 1961235: Experimental Crystal Structure Determination
CCDC 1961235: Experimental Crystal Structure Determination Open
View article: CCDC 1961236: Experimental Crystal Structure Determination
CCDC 1961236: Experimental Crystal Structure Determination Open
View article: CCDC 1961238: Experimental Crystal Structure Determination
CCDC 1961238: Experimental Crystal Structure Determination Open
View article: CCDC 1961234: Experimental Crystal Structure Determination
CCDC 1961234: Experimental Crystal Structure Determination Open
View article: CCDC 1961237: Experimental Crystal Structure Determination
CCDC 1961237: Experimental Crystal Structure Determination Open
View article: Ring-opening hydrolysis of spiro-epoxyoxindoles using a reusable sulfonic acid functionalized nitrogen rich carbon catalyst
Ring-opening hydrolysis of spiro-epoxyoxindoles using a reusable sulfonic acid functionalized nitrogen rich carbon catalyst Open
Catalytic synthesis of vicinal diols via ring-opening hydrolysis of spiro-epoxyoxindoles.
View article: Generation and application of Cu-bound alkyl nitrenes for the catalyst-controlled synthesis of cyclic β-amino acids
Generation and application of Cu-bound alkyl nitrenes for the catalyst-controlled synthesis of cyclic β-amino acids Open
Copper-catalysed conditions have been developed for the chemoselective synthesis of cyclic β-amino acids.
View article: CCDC 1889960: Experimental Crystal Structure Determination
CCDC 1889960: Experimental Crystal Structure Determination Open
View article: CCDC 1889953: Experimental Crystal Structure Determination
CCDC 1889953: Experimental Crystal Structure Determination Open
View article: CCDC 1889962: Experimental Crystal Structure Determination
CCDC 1889962: Experimental Crystal Structure Determination Open
View article: CCDC 1889952: Experimental Crystal Structure Determination
CCDC 1889952: Experimental Crystal Structure Determination Open
View article: CCDC 1889957: Experimental Crystal Structure Determination
CCDC 1889957: Experimental Crystal Structure Determination Open
View article: CCDC 1889954: Experimental Crystal Structure Determination
CCDC 1889954: Experimental Crystal Structure Determination Open